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Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts

BACKGROUND/AIMS: Cholangiocytes are capable of reabsorbing bile salts from bile, but the pathophysiological significance of this process is unclear. To this end, we detected the expression and distribution of bile acid transport proteins in cholangiocytes from normal rat liver and analyzed the possi...

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Autores principales: Luo, Zhu-lin, Cheng, Long, Wang, Tao, Tang, Li-jun, Tian, Fu-zhou, Xiang, Ke, Cui, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743800/
https://www.ncbi.nlm.nih.gov/pubmed/30919600
http://dx.doi.org/10.5009/gnl18265
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author Luo, Zhu-lin
Cheng, Long
Wang, Tao
Tang, Li-jun
Tian, Fu-zhou
Xiang, Ke
Cui, Lin
author_facet Luo, Zhu-lin
Cheng, Long
Wang, Tao
Tang, Li-jun
Tian, Fu-zhou
Xiang, Ke
Cui, Lin
author_sort Luo, Zhu-lin
collection PubMed
description BACKGROUND/AIMS: Cholangiocytes are capable of reabsorbing bile salts from bile, but the pathophysiological significance of this process is unclear. To this end, we detected the expression and distribution of bile acid transport proteins in cholangiocytes from normal rat liver and analyzed the possible pathophysiological significance. METHODS: Bile duct tissues of Sprague-Dawley rats were isolated by enzymatic digestion and mechanical isolation, and then divided into large and small bile duct tissues. Immunohistochemistry, real-time polymerase chain reaction and Western blotting were used to determine the expression of the apical sodium-dependent bile acid transporter (ASBT), ileal bile acid binding protein (IBABP), and basolateral organic solute transporter α (Ostα) in the biliary tract system of rats. Differences in the expression and distribution of these proteins were analyzed. RESULTS: In cholangiocytes, ASBT and IBABP were mainly expressed in cholangiocytes of the large bile ducts, in which the expression of both was significantly higher than that in the small ducts (p<0.05). Ostα was simultaneously expressed in cholangiocytes of both the large and small bile ducts, showing no significant difference in expression between the two groups of bile ducts (p>0.05). CONCLUSIONS: Bile acid transporters are expressed and heterogeneously distributed in rat bile ducts, indicating that bile acid reabsorption by cholangiocytes might mainly occur in the large bile ducts. These findings may help explore the physiology of bile ducts and the pathogenesis of various cholangiopathies.
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spelling pubmed-67438002019-09-20 Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts Luo, Zhu-lin Cheng, Long Wang, Tao Tang, Li-jun Tian, Fu-zhou Xiang, Ke Cui, Lin Gut Liver Original Article BACKGROUND/AIMS: Cholangiocytes are capable of reabsorbing bile salts from bile, but the pathophysiological significance of this process is unclear. To this end, we detected the expression and distribution of bile acid transport proteins in cholangiocytes from normal rat liver and analyzed the possible pathophysiological significance. METHODS: Bile duct tissues of Sprague-Dawley rats were isolated by enzymatic digestion and mechanical isolation, and then divided into large and small bile duct tissues. Immunohistochemistry, real-time polymerase chain reaction and Western blotting were used to determine the expression of the apical sodium-dependent bile acid transporter (ASBT), ileal bile acid binding protein (IBABP), and basolateral organic solute transporter α (Ostα) in the biliary tract system of rats. Differences in the expression and distribution of these proteins were analyzed. RESULTS: In cholangiocytes, ASBT and IBABP were mainly expressed in cholangiocytes of the large bile ducts, in which the expression of both was significantly higher than that in the small ducts (p<0.05). Ostα was simultaneously expressed in cholangiocytes of both the large and small bile ducts, showing no significant difference in expression between the two groups of bile ducts (p>0.05). CONCLUSIONS: Bile acid transporters are expressed and heterogeneously distributed in rat bile ducts, indicating that bile acid reabsorption by cholangiocytes might mainly occur in the large bile ducts. These findings may help explore the physiology of bile ducts and the pathogenesis of various cholangiopathies. Editorial Office of Gut and Liver 2019-09 2019-05-30 /pmc/articles/PMC6743800/ /pubmed/30919600 http://dx.doi.org/10.5009/gnl18265 Text en Copyright © 2019 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Luo, Zhu-lin
Cheng, Long
Wang, Tao
Tang, Li-jun
Tian, Fu-zhou
Xiang, Ke
Cui, Lin
Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts
title Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts
title_full Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts
title_fullStr Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts
title_full_unstemmed Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts
title_short Bile Acid Transporters Are Expressed and Heterogeneously Distributed in Rat Bile Ducts
title_sort bile acid transporters are expressed and heterogeneously distributed in rat bile ducts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743800/
https://www.ncbi.nlm.nih.gov/pubmed/30919600
http://dx.doi.org/10.5009/gnl18265
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